3-Fluoro-dl-phenylalanine

• CAS: 456-88-2
• Catalog Number: ACM456882
• Category: Other Products
• Molecular Weight: 183.18
• Molecular Formula: C₉H₁₀FNO₂
• Synonyms: M-FLUORO-DL-PHENYLALANINE;H-DL-PHE(3-F)-OH;H-M-FLUORO-DL-PHE-OH;DL-M-FLUOROPHENYLALANINE;2-AMINO-3-(3-FLUOROPHENYL)PROPIONIC ACID;3-FLUORO-DL-PHENYLALANINE;3-fluoro-3-phenylalanine ;2-amino-3-(3-fluorophenyl)propanoic acid
• Melting Point: ~240°C (dec.)
• Hazard Statements: Xi
• Safety Description: 24/25

Custom Q&A

What is the IUPAC name of the compound?

The IUPAC name of the compound is 2-amino-3-(3-fluorophenyl)propanoic acid.

What is the molecular formula of the compound?

The molecular formula of the compound is C9H10FNO2.

What is the molecular weight of the compound?

The molecular weight of the compound is 183.18 g/mol.

What is the CAS number of the compound?

The CAS number of the compound is 456-88-2.

What is the XLogP3 value of the compound?

The XLogP3 value of the compound is -1.9.

How many hydrogen bond donor count does the compound have?

The compound has 2 hydrogen bond donor count.

How many hydrogen bond acceptor count does the compound have?

The compound has 4 hydrogen bond acceptor count.

How many rotatable bond count does the compound have?

The compound has 3 rotatable bond count.

What is the topological polar surface area of the compound?

The topological polar surface area of the compound is 63.3 ?2.

Is the compound canonicalized?

Yes, the compound is canonicalized.

Synthetic Use

Upstream Synthesis Route 1

• 380-70-1

• 456-88-2

Reference: [1] European Journal of Medicinal Chemistry, 2018, vol. 143, p. 1325 - 1344
[2] Journal of the American Chemical Society, 1950, vol. 72, p. 1806
[3] Organic Letters, 2018, vol. 20, # 19, p. 6298 - 6301

Upstream Synthesis Route 2

• 207910-83-6

• 456-88-2

Reference: [1] Organic and Biomolecular Chemistry, 2004, vol. 2, # 18, p. 2684 - 2691

Upstream Synthesis Route 3

• 456-42-8

• 456-88-2

Reference: [1] Organic and Biomolecular Chemistry, 2004, vol. 2, # 18, p. 2684 - 2691

Upstream Synthesis Route 4

• 143051-43-8

• 456-88-2

Reference: [1]Journal of the American Chemical Society,1950,vol. 72,p. 1806

Upstream Synthesis Route 5

• 17607-28-2

• 456-88-2

Reference: [1]Journal of the American Chemical Society,1950,vol. 72,p. 1806

Downstream Synthesis Route 1

• 456-88-2

• 404-70-6

Reference: [1]Journal fur praktische Chemie (Leipzig 1954),1932,vol. <2> 135,p. 101,113

* For details of the synthesis route, please refer to the original source to ensure accuracy.